Laura Ashley Albany Table Lamp Recall [UK]

UK TSI RecallUK/Basildon: Laura Ashley recalls some Albany Table Lamps due to electric shock hazard. TSI: http://ht.ly/lvAsw

Direct link: http://www.tradingstandards.gov.uk/advice/advice-recall-item.cfm?id=302870

Laura Ashley LampAdditional information:
The Trading Standards Institute (“TSI”) reports this Table Lamp poses an electric shock hazard if the transformer plug cover becomes detached whilst plugged into any live electrical outlet.

Recalls Direct RIN: 2013-2045
About the Recalls Direct service: http://wp.me/P2bVty-2
Visit the Living Safely site: http://www.LivingSafely.org
E. & O. E.

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NHTSA May Vehicle Recalls – 58 MTD [US]

FlagUSUS/Washington: As of Wednesday, May 29, the US National Highway Traffic Safety Administration has posted 58 vehicle or tire recalls so far this month. Are yours listed? http://ht.ly/5G8bb

Direct link: http://www-odi.nhtsa.dot.gov/owners/SearchCurrentMonthRecall

Additional information:
Recently added recalls include products from the following manufacturers:

  • Brammo, Inc. – Electrical system: Potential Number of Units Affected: 5
  • Elite Trailer Manufacturing – Brake hazards: Potential Number of Units Affected: 9
  • Blue Bird Body Company – Seats: Potential Number of Units Affected: 441
  • Forest River, Inc. – Awning Motor: Potential Number of Units Affected: 9,526
  • Isuzu Manufacturing Services of America – Power train: Potential Number of Units Affected: 196
  • Pierce Manufacturing – Structural hazards: Potential Number of Units Affected: 1,965

Recalls Direct RIN: 2013-2043
About the Recalls Direct service: http://wp.me/P2bVty-2
Visit the Living Safely site: http://www.LivingSafely.org/
E. & O. E.

Main Street Family Pharmacy Compounded Product Recall [US]

United States FlagUS/Silver Spring: Main Street Family Pharmacy of Newbern, Tennessee recalls all lots of All Sterile Products compounded by the pharmacy due to microbial hazard. FDA: http://ht.ly/lvlik

Direct link: http://www.fda.gov/Safety/Recalls/ucm354182.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the Compounded Products subject to this recall are those products with a Use By Date on or before November 20, 2013. The recall was initiated after seven (7) reported cases of adverse events in the form of skin abscesses, one of which appears to be fungal in nature. An investigation into the exact source of the adverse events remains ongoing.

Recalls Direct RIN: 2013-2044
About the Recalls Direct service: http://wp.me/P2bVty-2
Visit the Living Safely site: http://www.LivingSafely.org
E. & O. E.

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